Leprot Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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15 records found for search term Leprot

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15138195	CV732563	single nucleotide variant	NM_017526.5(LEPROT):c.16+700G>A	not provided [RCV000898937]	likely benign	1	65421440	65421440	Human		name
11590057	CV282920	single nucleotide variant	NM_017526.5(LEPROT):c.21C>T (p.Leu7=)	Monogenic Non-Syndromic Obesity [RCV000397005]\|Obesity due to leptin receptor gene deficiency [RCV000315592]\|not provided [RCV000953426]	benign\|likely benign\|uncertain significance	1	65425307	65425307	Human	2	name
156272386	CV2195310	single nucleotide variant	NM_017526.5(LEPROT):c.22G>A (p.Val8Met)	not specified [RCV004080233]	uncertain significance	1	65425308	65425308	Human		name
156378104	CV2207632	single nucleotide variant	NM_017526.5(LEPROT):c.94G>A (p.Val32Ile)	not specified [RCV004090410]	uncertain significance	1	65429863	65429863	Human		name
597640981	CV3696046	single nucleotide variant	NM_017526.5(LEPROT):c.65T>C (p.Met22Thr)	not specified [RCV004941636]	uncertain significance	1	65425351	65425351	Human		name
155904481	CV2298813	single nucleotide variant	NM_017526.5(LEPROT):c.230T>C (p.Ile77Thr)	not specified [RCV004156365]	uncertain significance	1	65429999	65429999	Human		name
401893572	CV2763679	single nucleotide variant	NM_017526.5(LEPROT):c.199C>T (p.Arg67Trp)	not specified [RCV004343181]	uncertain significance	1	65429968	65429968	Human		name
407481302	CV3452719	single nucleotide variant	NM_017526.5(LEPROT):c.112G>A (p.Val38Ile)	not specified [RCV004642360]	uncertain significance	1	65429881	65429881	Human		name
156104905	CV2260616	single nucleotide variant	NM_015344.3(LEPROTL1):c.22A>G (p.Ile8Val)	not specified [RCV004123378]	uncertain significance	8	30101903	30101903	Human		name
407491986	CV3452720	single nucleotide variant	NM_015344.3(LEPROTL1):c.93C>A (p.Asn31Lys)	not specified [RCV004642361]	uncertain significance	8	30104300	30104300	Human		name
401868979	CV2767397	single nucleotide variant	NM_015344.3(LEPROTL1):c.230T>C (p.Ile77Thr)	not specified [RCV004349554]	uncertain significance	8	30104437	30104437	Human		name
597640994	CV3696048	single nucleotide variant	NM_015344.3(LEPROTL1):c.146A>G (p.Tyr49Cys)	not specified [RCV004941638]	uncertain significance	8	30104353	30104353	Human		name
126908720	CV969928	single nucleotide variant	NM_015344.3(LEPROTL1):c.193G>A (p.Ala65Thr)	Hereditary breast ovarian cancer syndrome [RCV001374542]	uncertain significance	8	30104400	30104400	Human	1	name
156316598	CV2193079	single nucleotide variant	NM_001128208.2(LEPROTL1):c.297C>A (p.Phe99Leu)	not specified [RCV004069623]	uncertain significance	8	30137289	30137289	Human		name
156181536	CV2384082	single nucleotide variant	NM_001128208.2(LEPROTL1):c.287G>A (p.Arg96His)	not specified [RCV004225443]	uncertain significance	8	30137279	30137279	Human		name